Freedom EVO 200 — Class II medical device recall Z-1851-2019
Terminated recall by Tecan US, Inc., reported 2019-07-03, distributed nationwide. Gas springs not always replaced within the interval specified.
| Recall number | Z-1851-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Tecan US, Inc., Morrisville, NC, United States |
| Recall initiated | 2019-04-12 |
| Classified | 2019-06-21 |
| Reported by FDA | 2019-07-03 |
| Terminated | 2022-01-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 40 |
| Serial numbers | 1004001243, 1006000274, 1006009336, 1009002730, 1011003146, 1011004081, 1011004086, 1011004089, 1011004095, 1104000151, 1108006349, 1108006724, 1108006777, 1109000886, 1109001036, 1109006938, 1111008689, 1203005259, 222, 506000013, 511000005, 603000004, 702, 702000004, 703000002 and 15 more |
Product
Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks, such as general purpose pipetting and general purpose liquid handling and robotic processes.
Reason for recall
Gas springs not always replaced within the interval specified.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1851-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.